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|Authors:||Damato, Pierre Jean|
Pace Balzan, J.
|Keywords:||Chordoma -- Malta -- Case studies|
Chordoma -- Etiology
Central nervous system -- Tumors
|Publisher:||The St. Luke`s Hospital Gazette|
|Citation:||Damato, P.J., & Pace Balzan, J. (1974). Parapharyngeal chordoma. The St. Luke`s Hospital Gazette, 9(2), 116-118.|
|Abstract:||Chordomas are rare tumours constituting less than one percent of all neoplasms affecting the Central Nervous System. They are some of the few malignant tumours originating from vestigial embryonic tissue which retain primitive histological features. The purpose of this paper is to report an unusual case of a chordoma arising in the region of the foramen magnum and extending laterally to present as a parapharyngeal tumour. Symptomatology varies with the site of origin of the tumour, but pain is the earliest and most common presenting symptom. Treatment is usually surgical and incomplete because of bone involvement at the time of diagnosis. High dosage radiotherapy has occasionally been used to control tumour residue in bone and recurrences.|
|Appears in Collections:||TSLHG, Volume 9, Issue 2|
TSLHG, Volume 9, Issue 2
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|Parapharyngeal Chordoma.pdf||Published for the Consultant Staff Committee, St. Luke`s Hospital, Malta and the Medical and Dental Surgery Faculties of the Royal University of Malta.||217.01 kB||Adobe PDF||View/Open|
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